{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Dublin",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71142",
      "recalling_firm": "Smiths Medical Asd Inc",
      "address_1": "6250 Shier Rings Rd",
      "address_2": "N/A",
      "postal_code": "43016-1270",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to the states of KY, MN, NJ, UT, & WI.",
      "recall_number": "Z-1730-2015",
      "product_description": "Low Volume Extension Set, 72' w/Clamp FLL/MLL APV=1.3ml, STERILE, AND FLUID PATH NONPYROGENIC UNLESS PACKAGE IS DAMAGED OR OPENED. LATEX FREE, SINGLE USE Tyvek pouches, 10 per box, Smiths Medical ASD, Inc.    Used to administer fluid and drugs intravenously.",
      "product_quantity": "6,000 units",
      "reason_for_recall": "Smiths Medical has become aware of an issue with the Low Volume Extension Set, (72'' Extension Set) where under-sized tubing was used in the production of 1 lot of product.",
      "recall_initiation_date": "20150504",
      "center_classification_date": "20150608",
      "termination_date": "20160120",
      "report_date": "20150617",
      "code_info": "Product Reorder Number: 537235C; Lot #2761409"
    }
  ]
}